Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.34 (C)
Location

Chromosome 14:27039812 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60892220, rs17212295

This variant has 2 HGVS names - click the plus to show

14:g.27039812C>G
ENST00000552303.1:n.206-37426C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 transcript and has 6062 sample genotypes.

Variant displays